WO1996009347A2 - Polyolefine presentant des proprietes antistatiques permanentes et ne formant pas de buee, son procede de fabrication et son utilisation - Google Patents

Polyolefine presentant des proprietes antistatiques permanentes et ne formant pas de buee, son procede de fabrication et son utilisation Download PDF

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Publication number
WO1996009347A2
WO1996009347A2 PCT/EP1995/003576 EP9503576W WO9609347A2 WO 1996009347 A2 WO1996009347 A2 WO 1996009347A2 EP 9503576 W EP9503576 W EP 9503576W WO 9609347 A2 WO9609347 A2 WO 9609347A2
Authority
WO
WIPO (PCT)
Prior art keywords
polyolefin
polyamide
segment
dew
polyether
Prior art date
Application number
PCT/EP1995/003576
Other languages
German (de)
English (en)
Other versions
WO1996009347A3 (fr
Inventor
Marcel Janssens
Original Assignee
A. Schulman Plastics N.V.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by A. Schulman Plastics N.V. filed Critical A. Schulman Plastics N.V.
Priority to KR1019970701716A priority Critical patent/KR970706346A/ko
Priority to EP95933359A priority patent/EP0781308B1/fr
Priority to DE59508542T priority patent/DE59508542D1/de
Priority to JP08517125A priority patent/JP2000511208A/ja
Publication of WO1996009347A2 publication Critical patent/WO1996009347A2/fr
Publication of WO1996009347A3 publication Critical patent/WO1996009347A3/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18—Manufacture of films or sheets
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/20—Manufacture of shaped structures of ion-exchange resins
    • C08J5/22—Films, membranes or diaphragms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02—Homopolymers or copolymers of hydrocarbons
    • C08L25/04—Homopolymers or copolymers of styrene
    • C08L25/08—Copolymers of styrene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment

Definitions

  • Polyolefin with permanent antistatic and non-thawing properties process for its preparation and use
  • the invention relates to a polyolefin with permanent antistatic and / or non-thawing properties, a process for producing this polyolefin and the use of the polyolefin and a film which is produced from this polyolefin.
  • polyolefin films are that they become statically charged relatively quickly during processing and adhere to one another on account of this static charge, which makes further mechanical processing of such films and, for example, the opening of bags made from these films difficult.
  • antistatic agents which suppress the static charge of the products produced are added to the polyolefins before processing.
  • polyolefin films must be equipped with appropriate thaw-preventing agents.
  • thaw-preventing agents when used as packaging material, it is desirable that the packaged goods remain visible and clearly recognizable to the consumer through the packaging film. Films with these properties are also used for greenhouses, where it is also necessary that they retain their translucent properties permanently.
  • Antioxidants prevent the moisture in the packaging from condensing on the inside of the film surface and thus adversely affecting the transparency of the film. It is known from the prior art to use ethoxylated fatty acid amines with high molecular weights as such antistatic agents.
  • Fatty acid-containing substances which have a chain length of 12 to 18 carbon units and a degree of ethoxylation of about 2 mol per mol of the substance are particularly preferred.
  • stearates such as glycerol monostearate can also be used as further substances.
  • High-molecular, long-chain compounds in particular fatty acid esters, are also used as anti-thaw agents.
  • fatty acid esters for example, glycerol monooleate and sorbitol onolaurate are used in polyolefins for packaging films and polyglycerol esters in polyolefins for greenhouse films.
  • these substances have the
  • the technical object of the present invention is therefore to provide polyolefins which are superior to the correspondingly equipped polyolefins of the prior art. These polyolefins are said to be permanently antistatic and to prevent the formation of dew without these substances gradually diffusing to the surface of the film in films made from these polyolefins. The efflorescence of substances is said to can be avoided and the transparency of the film produced from the polyolefin is retained.
  • polyol 5 fm which is characterized in that it contains 20 to 50% by weight of a hydrophilic polyether block amide.
  • the polyether block amide has the formula I.
  • PA represents the polyamide segment
  • PE represents the polyether segment: and 10 ⁇ . n . ⁇ . Is 60.
  • polyamides can be selected from the group polyamide 6; Polyamide 6.6; Polyamide 11; Polyamide 12; Polyamide 6.12; Polyamide 6, 11 or mixtures thereof may be included.
  • polystyrene block amides The use of such polyether block amides is possible with very different polyolefins.
  • the polyolefin can be low-density polyethylene, linear low-density polyethylene or also conventional polyethylene, polypropylene homopolymer, polypropylene block copolymer, polypropylene random copolymer, ethylene-vinyl acetate copolymer, polybutylene and polymethylpentene or a mixture thereof his.
  • a polyether block amide is particularly preferred which comprises polyamide 12 as the polyamide segment and the IC segment of the formula II as the polyether segment
  • the polyolefins according to the invention can also contain 1 to 20% by weight of a polyolefin resin, polyolefin elastomer or styrene elastomer as an additive, these substances preferably containing 0.1 to 5% maleic anhydride.
  • the compounds containing maleic anhydride are polypropylene resins, ethylene-propylene elastomer, linear low-density polyethylene or a styrene-isoprene-styrene elastomer.
  • the polyolefins according to the invention are prepared by compounding the individual constituents in a ZSK 30 twin-screw compounder at 180 to 240 ° C. After melting, the mixture is cooled in a water bath and optionally granulated. The granules so produced
  • 35 can then be converted into foils of any thickness, extruded into profiles or into finished articles. particles are injection molded.
  • compositions can be produced which contain 70% by weight of polypropylene and 30% by weight of polyether block. These have excellent permanent antistatic properties and are particularly suitable for injection molding.
  • a composition of 60% by weight polypropylene and 40% by weight polyether block amide is preferably used to produce films. Such films have excellent, long-lasting anti-static and anti-thaw properties.
  • the mechanical properties of such films or moldings can be further improved by adding polyolefin resin or polyolefin elastomers which contain maleic anhydride in an amount of 0.1 to 5% by weight. 5 to 15% by weight of a polypropylene containing maleic anhydride or 5 to 15% by weight of ethylene propylene elastomer containing maleic anhydride are preferably added, an amount of 10% by weight being particularly preferred.
  • the amide is incorporated into the polyethylene or polypropylene matrix, which surprisingly improves the processing of a corresponding polyolefin, as well as the mechanical properties of the finished products, in particular the impact resistance.
  • a typical application for such polyolefins are, for example, so-called biaxially oriented polypropylene films, the polyolefin according to the invention being introduced into the outer layer of a coextruded multilayer film during extrusion.
  • a film is obtained which has a particularly good sealability, has excellent optical and antistatic properties and shows no diffusion of the additives onto the surface of the film.
  • the inventive po Lyolefin is therefore considerably superior to the similar antistatic and / or polyolefins which are known from the prior art.
  • the polyolefins according to the invention can also be used, for example, to produce moldings, films and extrusion products based on low-density polyethylene, linear low-density polyethylene and ethylene-vinyl acetate copolymer. These materials are just as suitable for extrusion processes as for injection molding. The products made from these base materials also have excellent antistatic and non-dew forming properties.
  • polyolefin of the invention can be more ideal
  • Table 1 shows the composition of the polypropylenes.
  • Comparative examples 1 and 2 contain polypropylenes of the prior art which contain previously known antistatic agents and anti-thaw agents, namely ethoxylated fatty acid amines. In Examples 1 to 8, these were replaced by the polyether block amide according to the invention.
  • Biaxially oriented polypropylene films (boPP films) and moldings are produced from these polypropylenes.
  • boPP films with a wall thickness of 20 ⁇ m and in Examples 4 to 8 compositions for injection molding were produced .
  • the surface resistance in ohms, the charge drop in seconds, the surface properties and the Izod impact strength in J / m were determined for these individual products.
  • PP polypropylene
  • Atmer glycerol monostearate
  • EP ethylene - propylene
  • V comparative example
  • the surface resistance was measured in ohms. The digits indicate the base 10 exponent.
  • G greasy
  • B bloomed
  • C pure
  • the films produced from these polyolefins are subjected to a cold fog test to compare their properties. Films with a thickness of approximately 30 ⁇ m are produced. These foils are fixed over an open glass container that is filled with water at a height of 1 cm and placed in a refrigerator. The formation of dew is observed as a function of time. A bad film shows immediate dew formation on the inside of the film facing the water. A good film for packaging purposes shows no thawing for at least four weeks.
  • Table 2 shows the composition and properties of the films examined. Table 2
  • Films were subsequently produced from the polyolefins according to the invention having a composition according to Table 3 for use in greenhouses.
  • a film with a thickness of 180 ⁇ m was produced with a length of 1 and a width of 30 cm. With these foils a
  • Air humidity is set to 100% and the outside temperature is 21 "C.
  • the frame open at the bottom with the film stretched thereon is placed over a container with water, the water temperature being between 21 and 34 ° C, around the temperatures of one day and a night cycle, which is 12 hours each, a bad film shows blooming, which is undesirable because it reduces the light transmission of the film, and a bad film shows dew formation in a period of less than a week
  • a good film shows no blooming and an anti-thaw effect for a minimum time of 6 months, which corresponds to a durability of the anti-thaw properties of 3 cultivation periods
  • Table 3 The composition and properties of the films are summarized in Table 3 below.
  • LLDPE linear low density polyethylene
  • EVA-14% ethylene-vinyl acetate copolymer with 14 vinyl acetate
  • the polyolefins composed according to the invention with a proportion of polyether block amides are considerably superior to the polyolefins finished with the usual polyglycerol esters and have better surface properties and anti-thaw properties.
  • the film, produced from the composition according to Comparative Example 5 with polyglycerol ester shows an initial blooming after only one month.
  • the film made with polyether block amides shows no blooming even after 8 months.
  • the films produced from the polyolefin according to the invention are therefore considerably superior to those of the prior art in terms of their antistatic and non-dew-forming properties.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
  • Graft Or Block Polymers (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)
  • Laminated Bodies (AREA)

Abstract

L'invention concerne une polyoléfine présentant des propriétés antistatiques permanentes et/ou ne formant pas de buée, contenant 20 à 50 % en poids d'un polyéther-amide bloc hydrophile. L'invention concerne également un procédé de fabrication de cette polyoléfine ainsi que son utilisation pour la fabrication de feuilles de polyoléfine présentant des propriétés antistatiques améliorées et ne formant pas de buée.
PCT/EP1995/003576 1994-09-15 1995-09-12 Polyolefine presentant des proprietes antistatiques permanentes et ne formant pas de buee, son procede de fabrication et son utilisation WO1996009347A2 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
KR1019970701716A KR970706346A (ko) 1994-09-15 1995-09-12 영구히 지속되는 정전기 방지와 김서림 방지의 성질을 가진 폴리올레핀, 그의 제조방법 및 그의 용도
EP95933359A EP0781308B1 (fr) 1994-09-15 1995-09-12 Polyolefine presentant des proprietes antistatiques permanentes et ne formant pas de buee, son procede de fabrication et son utilisation
DE59508542T DE59508542D1 (de) 1994-09-15 1995-09-12 Polyolefin mit permanenten antistatischen und nicht-taubildenden eigenschaften, verfahren zu seiner herstellung und seine verwendung
JP08517125A JP2000511208A (ja) 1994-09-15 1995-09-12 永久帯電防止性及び防曇性を持つポリオレフィン、その製造方法、並びにその使用

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4432777A DE4432777C1 (de) 1994-09-15 1994-09-15 Polyolefin mit permanenten antistatischen und nicht-taubildenden Eigenschaften, Verfahren zu seiner Her stellung und seine Verwendung
DEP4432777.3 1994-09-15

Publications (2)

Publication Number Publication Date
WO1996009347A2 true WO1996009347A2 (fr) 1996-03-28
WO1996009347A3 WO1996009347A3 (fr) 1996-07-25

Family

ID=6528229

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Application Number Title Priority Date Filing Date
PCT/EP1995/003576 WO1996009347A2 (fr) 1994-09-15 1995-09-12 Polyolefine presentant des proprietes antistatiques permanentes et ne formant pas de buee, son procede de fabrication et son utilisation

Country Status (7)

Country Link
EP (1) EP0781308B1 (fr)
JP (1) JP2000511208A (fr)
KR (1) KR970706346A (fr)
DE (2) DE4432777C1 (fr)
ES (1) ES2151081T3 (fr)
TW (1) TW434290B (fr)
WO (1) WO1996009347A2 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2332390A (en) * 1997-12-19 1999-06-23 Hoechst Trespaphan Gmbh Polymeric films
EP1273425A1 (fr) * 2001-07-06 2003-01-08 Huhtamaki France S.A. Structure multicouche pour le conditionnement de produits alimentaires et procédé de fabrication de ladite structure

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU5592301A (en) * 2000-07-24 2002-01-31 Yupo Corporation Label for in-mold decorating and labeled resin molded article
ATE518909T1 (de) * 2003-05-17 2011-08-15 Schulman A Plastics Polypropylenionomere für folien mit antistatischen und/oder nicht taubildenden eigenschaften
JP4526937B2 (ja) * 2004-12-02 2010-08-18 アキレス株式会社 半導体製造テープ用帯電防止基材フィルム
CN114437438B (zh) * 2020-10-30 2023-09-08 中国石油化工股份有限公司 一种永久抗静电聚乙烯组合物及其制备方法和应用

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2112789A (en) * 1981-12-29 1983-07-27 Ato Chimie New polyolefins based compositions

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07108972B2 (ja) * 1984-04-16 1995-11-22 東レ株式会社 防曇・防滴処理剤
JP2570258B2 (ja) * 1986-02-04 1997-01-08 東レ株式会社 植物栽培用ハウス
CH671022A5 (fr) * 1986-08-26 1989-07-31 Inventa Ag
JP3181681B2 (ja) * 1992-04-17 2001-07-03 三洋化成工業株式会社 樹脂組成物

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2112789A (en) * 1981-12-29 1983-07-27 Ato Chimie New polyolefins based compositions

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch, Week 8550 Derwent Publications Ltd., London, GB; Class A82, AN 85-314135 & JP,A,60 219 285 (TORAY IND) , 1.November 1985 *
DATABASE WPI Section Ch, Week 8737 Derwent Publications Ltd., London, GB; Class A97, AN 87-260391 & JP,A,62 179 938 (TORAY IND) , 7.August 1987 *
DATABASE WPI Section Ch, Week 9349 Derwent Publications Ltd., London, GB; Class A17, AN 93-392823 & JP,A,05 295 191 (SANYO CHEM IND) , 9.November 1993 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2332390A (en) * 1997-12-19 1999-06-23 Hoechst Trespaphan Gmbh Polymeric films
EP1273425A1 (fr) * 2001-07-06 2003-01-08 Huhtamaki France S.A. Structure multicouche pour le conditionnement de produits alimentaires et procédé de fabrication de ladite structure
FR2826908A1 (fr) * 2001-07-06 2003-01-10 Polarcup France Sa Structure multicouche pour le conditionnement de produit et procede de fabrication de ladite structure

Also Published As

Publication number Publication date
KR970706346A (ko) 1997-11-03
DE4432777C1 (de) 1996-02-29
EP0781308B1 (fr) 2000-07-05
WO1996009347A3 (fr) 1996-07-25
TW434290B (en) 2001-05-16
EP0781308A2 (fr) 1997-07-02
DE59508542D1 (de) 2000-08-10
ES2151081T3 (es) 2000-12-16
JP2000511208A (ja) 2000-08-29

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